Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 Biomarker disease CTD_human
Entrez Id: 79140
Gene Symbol: CCDC28B
CCDC28B 		0.500 Biomarker disease CTD_human
Entrez Id: 27241
Gene Symbol: BBS9
BBS9 		0.400 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 79738
Gene Symbol: BBS10
BBS10 		0.400 GeneticVariation disease CLINVAR
Entrez Id: 79738
Gene Symbol: BBS10
BBS10 		0.400 CausalMutation disease CLINVAR
Entrez Id: 8195
Gene Symbol: MKKS
MKKS 		0.400 CausalMutation disease CLINVAR
Entrez Id: 27241
Gene Symbol: BBS9
BBS9 		0.400 CausalMutation disease CLINVAR
Entrez Id: 79738
Gene Symbol: BBS10
BBS10 		0.400 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 51057
Gene Symbol: WDPCP
WDPCP 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 55212
Gene Symbol: BBS7
BBS7 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 129880
Gene Symbol: BBS5
BBS5 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 583
Gene Symbol: BBS2
BBS2 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 84100
Gene Symbol: ARL6
ARL6 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 166379
Gene Symbol: BBS12
BBS12 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 585
Gene Symbol: BBS4
BBS4 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 Biomarker disease BEFREE Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1). 10564830 1999
Entrez Id: 10938
Gene Symbol: EHD1
EHD1 		0.010 Biomarker disease BEFREE EHD1, a new member of the EH-domain containing proteins, was identified in this study as lying within the BBS1 disease interval. 10564830 1999
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 Biomarker disease BEFREE Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees. 10577921 1999
Entrez Id: 8195
Gene Symbol: MKKS
MKKS 		0.400 Biomarker disease GENOMICS_ENGLAND Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome. 10802661 2000
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 Biomarker disease GENOMICS_ENGLAND Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder. 11567139 2001
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 CausalMutation disease CLINVAR Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. 12118255 2002
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 GeneticVariation disease UNIPROT Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. 12118255 2002
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.940 Biomarker disease GENOMICS_ENGLAND Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. 12118255 2002
Entrez Id: 254359
Gene Symbol: ZDHHC24
ZDHHC24 		0.100 CausalMutation disease CLINVAR Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. 12118255 2002